Abstract

Electrolysis of Co(2+) in phosphate, methylphosphonate, and borate electrolytes effects the electrodeposition of an amorphous highly active water oxidation catalyst as a thin film on an inert anode. Electrodeposition of a catalytically competent species immediately follows oxidation of Co(2+) to Co(3+) in solution. Methylphosphonate and borate electrolytes support catalyst activity comparable to that observed for phosphate. Catalytic activity for O(2) generation in aqueous solutions containing 0.5 M NaCl is retained for catalysts grown from phosphate electrolyte.

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